ClearanceBrief
510(k) K850061 ยท FPA Set, Administration, Intravascular

MICRO VOLUME DOUBLE LINE EXTENSION SET

ApplicantTravenol Laboratories, S.A., Hooksett NH, US
DecisionSubstantially Equivalent, Mar 27, 1985
ReceivedJan 8, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850061

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.